Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 26161–26180 of 27,462 recalls
Recalled Item: MEDRAD Hand Controller Sheath Recalled by Medrad Inc Due to The seal between...
The Issue: The seal between the white polyethylene and the clear plastic may be missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Skull Clamps Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniGuide BP-ROBOTIC ( BeamPath Robotic) Recalled by OmniGuide, Inc. Due to...
The Issue: Failure of glue joint, allowed a portion of the single use device to shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are...
The Issue: The BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Trauma Nail System. The devices are indication for bone fixation....
The Issue: Recall was initiated due to the possibility that the outer pouch was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...
The Issue: Additional Warning Statement to prevent burns to the skin
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Analyzer Series Recalled by Roche Diagnostics Operations,...
The Issue: On cobas c 701 and cobas c 702 modules of the Cobas 8000 series analyzer, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Reamer Sleeve KNEE REAMER SLEEVE 13.0 thru 20.0 Recalled by Biomet, Inc....
The Issue: Biomet has initiated this action following an investigation which identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to It has...
The Issue: It has been determined that, in some cases, pulley drive components have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Modular Humeral Head 48mm x 24mm Ti 6AI4V/Ion Implanted (Orthopedic...
The Issue: The items in this lot are missing the ion implantation feature. The surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.